RIVA, PAOLA VANDA

RIVA, PAOLA VANDA  

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale  

Risultati 1 - 20 di 93 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autore(i) Tipo File Abstract
19p deletion in recurring leiomyosarcoma lesions from the same patient 1-giu-2000 P. RivaV. GualandriM. VolontèM. MiozzoA. F. ContiL. Larizza + Article (author) -
1p36 LOH and expression study of apoptotic genes in a selected group of chordomas 1-gen-2006 M. StroppiP. Riva + Article (author) -
The 3' untranslated region of human cyclin-dependent kinase 5 regulatory subunit 1 contains regulatory elements affecting transcript stability 3-dic-2007 S. MonciniA. BevilacquaM. VenturinA. RattiA. NicolinP. Riva + Article (author) -
A 12-bp deletion (7818del12) in the c-kit protooncogene in a large Italian kindred with piebaldism 1-gen-1995 P. RivaL. Larizza + Article (author) -
A novel potentially diagnostic polymorphism (4894 A/C) in exon 10 of the human c-kit proto-oncogene 1-ott-1996 P. RivaL. Larizza Article (author) -
A tandem duplication of chromosome 21 in a newborn showing a phenotype inconsistent with Down syndrome 1-apr-2010 E. MartinoliG.V. ZuccottiM. VolontèM. VenturinP.V. Riva + Article (author) -
ADAP2 in heart development: a candidate gene for the occurrence of cardiovascular malformations in NF1 microdeletion syndrome 1-gen-2014 M. VenturinS. CarraG. GaudenziG.R. GalloS. MonciniF. CotelliP. Riva + Article (author) -
Breakpoint characterization of a novel NF1 multiexonic deletion : a case showing expression of the mutated allele 1-mag-2008 F. OrzanM. StroppiM. VenturinP. Riva + Article (author) -
Centaurin-α2 Interacts with β-Tubulin and Stabilizes Microtubules 1-dic-2012 P. ZuccottiD. CartelliV. PandiniM. VenturinA. AlivertiE. BattaglioliG. CappellettiP.V. Riva + Article (author) -
Characterization of a cytogenetic 17q11.2 deletion in an NF1 patient with a contiguous gene syndrome 1-dic-1996 P. RivaL. DonedaL. Larizza + Article (author) -
Characterization of a non-recurrent familial translocation t(7;9)(q11.23;p24.3) points to a recurrent involvement of the Williams-Beuren syndrome region in chromosomal rearrangements 1-gen-2006 M. VenturinA. PatriziMARTINOLI, EMANUELAP. Riva + Article (author) -
Chromosomal instability in Cancer : a genomic condition reflecting alterations of different cellular mechanisms 1-gen-2008 P. RivaLONGONI, MAURO Book Part (author) -
Chromosomal instability in fibroblasts and mesenchymal tumors from 2 sibs with Rothmund-Thomson syndrome 12-ago-1998 M. MiozzoP. RivaA. M. Fuhrman ContiL. VolpiL. Larizza + Article (author) -
Cromosomi umani 1-gen-2013 P.V. Riva Book Part (author) -
Current therapeutic options and novel molecular markers in skull base chordomas 1-gen-2012 P. Riva + Article (author) -
Developmental abnormalities and cancer predisposition in neurofibromatosis type 1 1-gen-2009 L. LarizzaC.C.G. GervasiniP.V. Riva + Article (author) -
Differential allelic expression of SOS1 and hyperexpression of the activating SOS1 c.755C variant in a Noonan syndrome family 1-gen-2015 S. MonciniI. MorellaL. FerrariP. Riva + Article (author) -
Differential allelic expression of the SOS1 c.755C activating variant in a Noonan syndrome family 1-mag-2014 S. MonciniL. FerrariP. Riva + Article (author) -
Digenic inheritance of subclinical variants in Noonan Syndrome patients: an alternative pathogenic model? 1-giu-2020 Ferrari L.Capitanio D.Gelfi C.Battaglia C.Riva P. + Article (author) -
The discovery of a new role of HDAC8 in skeletal muscle differentiation and in centronuclear myopathy insurgence 17-giu-2018 L. FerrariL. BrioschiS. EspositoM. MazzolaA. PezzottaP. RivaP. VianiG. CossuM. MoraA. MarozziA. Pistocchi + Conference Object -